- Establishment: CSIR-CDRI was established on February 17, 1951.
- Location: It is headquartered in Lucknow, Uttar Pradesh, India.
- Affiliation: It operates under the aegis of the Council of Scientific and Industrial Research (CSIR), India’s largest research and development organization.
Objectives
CSIR-CDRI aims to contribute to the development of new drugs and therapies for various diseases. Its objectives include:
- Discovering and developing new drugs and therapies.
- Conducting advanced research in the fields of biomedical sciences and pharmaceutical technology.
- Providing scientific and technical expertise in drug research.
For a government job opening at the Central Drug Research Institute (CDRI), the job role might involve a variety of responsibilities depending on the specific position. However, common roles at such institutes often include research, development, and regulatory compliance. Here’s a general outline of potential job roles and descriptions for a position at CDRI:
1. Research Scientist
- Research Design and Execution:
- Plan and conduct scientific experiments to advance drug development and discovery, focusing on pharmacology, toxicology, or other relevant areas.
- Develop and refine research protocols to investigate drug efficacy, safety, and mechanisms of action.
- Data Analysis and Reporting:
- Analyze experimental data using advanced statistical and computational methods.
- Prepare detailed research reports, publications, and presentations to disseminate findings to the scientific community.
- Collaboration:
- Work with multidisciplinary teams including biologists, chemists, and pharmacologists to integrate research efforts and achieve project objectives.
- Participate in collaborative research projects with other institutions and industry partners.
2. Clinical Research Coordinator
- Study Management:
- Oversee the planning, implementation, and monitoring of clinical trials, ensuring adherence to protocol and regulatory requirements.
- Coordinate with investigators, clinical staff, and regulatory bodies to facilitate smooth execution of clinical studies.
- Regulatory Compliance:
- Prepare and submit documentation for ethical review boards, regulatory agencies, and funding bodies.
- Ensure compliance with Good Clinical Practice (GCP) and other regulatory standards throughout the study lifecycle.
- Data Management:
- Manage and analyze clinical trial data, ensuring accuracy and integrity of information collected.
- Generate reports and assist in data interpretation to support decision-making and regulatory submissions.
3. Pharmacovigilance Specialist
- Safety Monitoring:
- Monitor and assess adverse drug reactions (ADRs) and safety profiles of investigational and marketed drugs.
- Report and document ADRs in accordance with regulatory guidelines and institute protocols.
- Risk Management:
- Develop and implement risk management strategies to mitigate potential safety issues related to drug products.
- Collaborate with regulatory agencies to address safety concerns and update product labeling as necessary.
- Regulatory Affairs:
- Ensure compliance with pharmacovigilance regulations and guidelines, including reporting to authorities such as the FDA or EMA.
- Prepare safety reports and contribute to the preparation of regulatory submissions and dossiers.
4. Medical Research Officer
- Project Oversight:
- Supervise and manage research projects focused on drug discovery, development, or disease mechanisms.
- Ensure alignment with research goals and regulatory requirements, and monitor project progress.
Research and Development
CSIR-CDRI conducts research in multiple areas, including:
- Synthetic Chemistry: Development of new synthetic methods and novel molecules for therapeutic use.
- Natural Products: Exploration of medicinal plants and natural products for potential drug leads.
- Pharmacology: Studying the biological effects of new drug candidates.
- Toxicology: Assessing the safety and toxicity profiles of new drug entities.
- Biotechnology: Applying biotechnological methods to discover and develop new drugs.
- Clinical Research: Conducting clinical trials to evaluate the efficacy and safety of new drugs.
- Neurobiology
- Virology
- Parasite Biology
- Endocrinology
- Human Genetics
- Analytical Biochemistry
- Computational Chemistry
- Medicinal Process Chemistry
- Statistics
- IPR & HR Management
Candidate Profile
- Strong academic credentials
- Proven track record of scientific achievements
- Motivation to engage in innovative research
- Alignment with the institute’s goals and national research missions
Contact Information
For more details on the application process, deadlines, and specific requirements, candidates are encouraged to visit the official CSIR-CDRI website or contact the institute’s Human Resources department directly.
Timing
Eligible candidates are required to report for the interview according to the following schedule:
- 03-06-2024: For Position Code No. 001 to 024 (Area of Chemical Sciences and Pharma)
- 05-06-2024: For Position Code No. 025 to 027 (Area of Life Sciences (Project Research Scientists))
- 06-06-2024: For Position Code No. 028 to 053 (Area of Life Sciences and S & T Management)
Interview Details:
- Time: From 09:00 AM onwards. Candidates reporting after 10:00 AM will not be entertained.
- Venue: CSIR-Central Drug Research Institute, Sector 10, Jankipuram Extension, Sitapur Road, Lucknow-226031.
Requirements:
- Eligible candidates must bring with them a duly filled application and undertaking. These forms can be downloaded from the CSIR-CDRI website.
- Candidates should also bring original and self-attested copies of mark sheets/certificates and a recent passport size photograph.
- Tentative mark sheets/certificates and ‘result awaited’ statuses will not be considered.
Eligiblity and Qualification
click here to view more details :- https://cdri.res.in/pdf/recruitment/advt022024.pdf
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